Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:126268775-126269232 | Common:14; Rare:1153; Clinvar:17; Clinvar (benign):34 | ||||
chr11:126282858-126283370 | Common:6; Rare:366 | ||||
chr11:126283468-126283787 | Rare:109 | ||||
chr11:126303586-126304740 | Common:19; Rare:1158; Clinvar:2 | ||||
chr11:126354930-126355330 | Rare:72 | ||||
chr11:126355411-126356405 | Common:16; Rare:828 | ||||
chr11:128522250-128522640 | Common:10; Rare:408 | ||||
chr11:129895425-129895825 | Common:17; Rare:489 | ||||
chr11:130002149-130002668 | Rare:387 | ||||
chr11:130002640-130003410 | Common:20; Rare:1031 | ||||
chr11:130069054-130069497 | Common:7; Rare:156 | ||||
chr11:130069535-130069970 | Common:10; Rare:654 | ||||
chr11:130070410-130071447 | Common:24; Rare:418 | ||||
chr11:130314227-130314629 | Common:8; Rare:495 | ||||
chr11:130314640-130315147 | Common:18; Rare:619 |